Preparation and Characterization of Novel disubstituted 1,3- Oxazepine tetra-one from Schiff bases reaction with 3-methylfuran-2,5-dione and 3- Phenyldihydrofuran-2,5-dione

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DC Field	Value	Language
dc.contributor.author	Abdul Kareem Hamad Ayfan, Rasim F. Muslim	-
dc.contributor.author	Noor Sabah Noori	-
dc.date.accessioned	2022-10-12T20:40:52Z	-
dc.date.available	2022-10-12T20:40:52Z	-
dc.date.issued	2019	-
dc.identifier.issn	0974-3618 (Print) 0974-360X (Online)	-
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/208	-
dc.description.abstract	This research includes synthesis of new heterocyclic derivatives of novel disubstituted 1,3- oxazepine-tetra-one from Schiff bases reaction with 3-methylfuran-2,5-dione and 3-phenyldihydrofuran-2,5-dione. Schiff bases [A1- A5] were synthesized by the reaction of aromatic aldehydes with primary aromatic amines, in the presence of glacial acetic acid as catalyst in absolute ethanol. The novel derivatives[A6-A10] were obtained from treatment of Schiff bases with anhydrides. The synthesized compounds were identified by TLC and via spectral methods, their (FT-IR, 1H-NMR and 13C-NMR) and measurements of some of its physical properties	en_US
dc.language.iso	en	en_US
dc.publisher	Research Journal of Pharmacy and Technology	en_US
dc.subject	1H-NMR	en_US
dc.subject	13C-NMR	en_US
dc.subject	TLC	en_US
dc.subject	Schiff bases	en_US
dc.subject	oxazepine-tetra-one	en_US
dc.title	Preparation and Characterization of Novel disubstituted 1,3- Oxazepine tetra-one from Schiff bases reaction with 3-methylfuran-2,5-dione and 3- Phenyldihydrofuran-2,5-dione	en_US
dc.type	Article	en_US
Appears in Collections:	قسم البيئة

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